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DNA methylation patterns in hereditary human cancers mimic sporadic tumorigenesis

Human molecular genetics, 2001-12, Vol.10 (26), p.3001-3007

2001

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Analysis of BRCA1 and BRCA2 mutations in Hungarian families with breast or breast-ovarian cancer

American journal of human genetics, 1997-05, Vol.60 (5), p.1242-1246

1997

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Idiopathic slow-transit constipation is not associated with mutations of the RET proto-oncogene or GDNF

Diseases of the colon & rectum, 2000-06, Vol.43 (6), p.851-857

2000

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Novel human, mouse and xenopus genes encoding a member of the RAS superfamily of low‐molecular‐weight GTP‐binding proteins and its downregulation in W/W V mouse jejunum

Journal of gastroenterology and hepatology, 2004-02, Vol.19 (2), p.211-217

2004

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The role of gene mutations in the genesis of familial cancers

The FASEB journal, 1993-07, Vol.7 (10), p.910-919

1993

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Transfection of rat ovarian surface epithelium with erb-B2/neu induces transformed phenotypes in vitro and the tumorigenic phenotype in vivo

The American journal of pathology, 1998-01, Vol.152 (1), p.297-306

1998

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RET oncogene

Current opinion in genetics & development, 1996-02, Vol.6 (1), p.82-86

1996

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The Drosophila Ret gene is transcribed in multiple alternatively spliced forms

Molecular & general genetics, 2000-10, Vol.264 (3), p.335-340

2000

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Inhibition of endogenous tissue alkaline phosphatase with the use of alkaline phosphatase conjugates in immunohistochemistry

The journal of histochemistry and cytochemistry, 1981-08, Vol.29 (8), p.981-984

1981

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Development of multiple endocrine neoplasia type 2A does not involve substantial deletions of chromosome 10

Genomics (San Diego, Calif.), 1989-04, Vol.4 (3), p.246-250

1989

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High allele loss rates at 17q12-q21 in breast and ovarian tumors from BRCAl-linked families. The Breast Cancer Linkage Consortium

Genes chromosomes & cancer, 1995-07, Vol.13 (3), p.203-210

1995

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Styl RFLP recognised by a human IRBP cDNA localised to chromosome 10

Nucleic acids research, 1988-02, Vol.16 (4), p.1645-1645

1988

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Immunohistochemical demonstration of H2 antigens in mouse tissue sections

The journal of histochemistry and cytochemistry, 1983-07, Vol.31 (7), p.911-919

1983

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Multifactorial Analysis of Differences Between Sporadic Breast Cancers and Cancers Involving BRCA1 and BRCA2 Mutations

JNCI : Journal of the National Cancer Institute, 1998-08, Vol.90 (15), p.1138-1145

1998

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Management of Extruded Porous High-density Polyethylene Implant in the Internal Nasal Valve

Plastic and reconstructive surgery. Global open, 2022-11, Vol.10 (11), p.e4647

2022

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Instability of short tandem repeats (microsatellites) in human cancers

Nature genetics, 1994-02, Vol.6 (2), p.152-156

1994

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Histopathology, FIGO Stage, and BRCA Mutation Status of Ovarian Cancers from the Gilda Radner Familial Ovarian Cancer Registry

International journal of gynecological pathology, 2004-01, Vol.23 (1), p.29-34

2004

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The Pathology of Familial Breast Cancer: Histological Features of Cancers in Families Not Attributable to Mutations in BRCA1 or BRCA2

Clinical cancer research, 2000-03, Vol.6 (3), p.782-789

2000

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Ovarian Carcinoma In Situ With Germline BRCA1 Mutation and Loss of Heterozygosity at BRCA1 and TP53

JNCI : Journal of the National Cancer Institute, 2000-07, Vol.92 (13), p.1088-1091

2000

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Pathology of familial breast cancer: differences between breast cancers in carriers of BRCA1 or BRCA2 mutations and sporadic cases

The Lancet (British edition), 1997-05, Vol.349 (9064), p.1505-1510

Stratton, Michael R

1997

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Deletion of genes on chromosome 1 in endocrine neoplasia

Nature (London), 1987-08, Vol.328 (6130), p.524-526

1987

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Genetic events in tumour initiation and progression in multiple endocrine neoplasia type 2

Genes chromosomes & cancer, 1993-03, Vol.6 (3), p.166-177

1993

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Comparative Study of Ovarian Cancer Histopathology by Registry Pathologists and Referral Pathologists: A Study by the Gilda Radner Familial Ovarian Cancer Registry

Gynecologic oncology, 2000-08, Vol.78 (2), p.166-170

2000

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Loss of NFI alleles in phaeochromocytomas from patients with type I neurofibromatosis

Genes chromosomes & cancer, 1992-01, Vol.4 (4), p.337-342

1992

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BclI RFLP for the human vimentin gene

Nucleic acids research, 1988-09, Vol.16 (18), p.9068-9068

1988

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DNA methylation patterns in hereditary human cancers mimic sporadic tumorigenesis

Analysis of BRCA1 and BRCA2 mutations in Hungarian families with breast or breast-ovarian cancer

Idiopathic slow-transit constipation is not associated with mutations of the RET proto-oncogene or GDNF

Novel human, mouse and xenopus genes encoding a member of the RAS superfamily of low‐molecular‐weight GTP‐binding proteins and its downregulation in W/W V mouse jejunum

The role of gene mutations in the genesis of familial cancers

Transfection of rat ovarian surface epithelium with erb-B2/neu induces transformed phenotypes in vitro and the tumorigenic phenotype in vivo

RET oncogene

The Drosophila Ret gene is transcribed in multiple alternatively spliced forms

Inhibition of endogenous tissue alkaline phosphatase with the use of alkaline phosphatase conjugates in immunohistochemistry

Development of multiple endocrine neoplasia type 2A does not involve substantial deletions of chromosome 10

High allele loss rates at 17q12-q21 in breast and ovarian tumors from BRCAl-linked families. The Breast Cancer Linkage Consortium

Styl RFLP recognised by a human IRBP cDNA localised to chromosome 10

Immunohistochemical demonstration of H2 antigens in mouse tissue sections

Multifactorial Analysis of Differences Between Sporadic Breast Cancers and Cancers Involving BRCA1 and BRCA2 Mutations

Management of Extruded Porous High-density Polyethylene Implant in the Internal Nasal Valve

Instability of short tandem repeats (microsatellites) in human cancers

Histopathology, FIGO Stage, and BRCA Mutation Status of Ovarian Cancers from the Gilda Radner Familial Ovarian Cancer Registry

The Pathology of Familial Breast Cancer: Histological Features of Cancers in Families Not Attributable to Mutations in BRCA1 or BRCA2

Ovarian Carcinoma In Situ With Germline BRCA1 Mutation and Loss of Heterozygosity at BRCA1 and TP53

Pathology of familial breast cancer: differences between breast cancers in carriers of BRCA1 or BRCA2 mutations and sporadic cases

Deletion of genes on chromosome 1 in endocrine neoplasia

Genetic events in tumour initiation and progression in multiple endocrine neoplasia type 2

Comparative Study of Ovarian Cancer Histopathology by Registry Pathologists and Referral Pathologists: A Study by the Gilda Radner Familial Ovarian Cancer Registry

Loss of NFI alleles in phaeochromocytomas from patients with type I neurofibromatosis

BclI RFLP for the human vimentin gene

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